Benzodiazepine use and mortality in chronic heart failure

INTRODUCTIONThe prognostic implications of using benzodiazepines (BZD) in heart failure (HF) patients are still unknown.OBJECTIVESThis study aimed to assess the association of BZD use with all‑cause death in ambulatory, chronic HF patients.PATIENTS AND METHODSWe investigated a retrospective cohort o...

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Veröffentlicht in:Polskie archiwum medycyny wewne̦trznej 2023-10, Vol.133 (10)
Hauptverfasser: Ribeirinho-Soares, Pedro, Madureira, Sérgio, Elias, Catarina, Gouveia, Rita, Neves, Ana, Amorim, Marta, Carreira, Marta S, Pereira, Joana, Almeida, Jorge, Lourenço, Patrícia
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container_issue 10
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container_title Polskie archiwum medycyny wewne̦trznej
container_volume 133
creator Ribeirinho-Soares, Pedro
Madureira, Sérgio
Elias, Catarina
Gouveia, Rita
Neves, Ana
Amorim, Marta
Carreira, Marta S
Pereira, Joana
Almeida, Jorge
Lourenço, Patrícia
description INTRODUCTIONThe prognostic implications of using benzodiazepines (BZD) in heart failure (HF) patients are still unknown.OBJECTIVESThis study aimed to assess the association of BZD use with all‑cause death in ambulatory, chronic HF patients.PATIENTS AND METHODSWe investigated a retrospective cohort of ambulatory HF patients with left ventricular systolic dysfunction (LVSD). The patients were followed up from their first medical appointment until January 2021 and all‑cause mortality was the primary end point. The Cox regression analysis was used to assess the association between BZD use and all‑cause mortality. Subgroup analyses were performed considering age, sex, body mass index (BMI), respiratory disease, chronic kidney disease (CKD), and New York Heart Association (NYHA) class. Multivariable models were built to account for confounders.RESULTSWe studied 854 patients (69% men), of mean (SD) age 71 (13) years, of whom 51% had severe LSVD, and 242 (28.3%) regularly used BZD. During a median follow‑up of 46 months, 443 patients (51.9%) died. BZD use predicted no crude survival disadvantage in the entire investigated group and in the subgroup analysis according to sex, respiratory disease, BMI, and NYHA class. BZD use was not mortality‑associated among patients aged 75 years and younger. However, in those older than 75 years the hazard ratio (HR) of all‑cause death was 1.3 (95% CI, 0.99-1.69; P = 0.06). BZD use seemed safe in the patients without CKD, but in those with CKD it was associated with worse survival (HR, 1.33; 95% CI, 1.02-1.73). In a multivariable‑adjusted analysis, the use of BZD was independently associated with increased death risk (HR, 1.36; 95% CI, 1.06-1.75).CONCLUSIONSThe patients medicated with BZD presented a 36% higher risk of dying. BZD should probably be used with caution, particularly in older HF patients and in those with CKD.
doi_str_mv 10.20452/pamw.16464
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The patients were followed up from their first medical appointment until January 2021 and all‑cause mortality was the primary end point. The Cox regression analysis was used to assess the association between BZD use and all‑cause mortality. Subgroup analyses were performed considering age, sex, body mass index (BMI), respiratory disease, chronic kidney disease (CKD), and New York Heart Association (NYHA) class. Multivariable models were built to account for confounders.RESULTSWe studied 854 patients (69% men), of mean (SD) age 71 (13) years, of whom 51% had severe LSVD, and 242 (28.3%) regularly used BZD. During a median follow‑up of 46 months, 443 patients (51.9%) died. BZD use predicted no crude survival disadvantage in the entire investigated group and in the subgroup analysis according to sex, respiratory disease, BMI, and NYHA class. BZD use was not mortality‑associated among patients aged 75 years and younger. However, in those older than 75 years the hazard ratio (HR) of all‑cause death was 1.3 (95% CI, 0.99-1.69; P = 0.06). BZD use seemed safe in the patients without CKD, but in those with CKD it was associated with worse survival (HR, 1.33; 95% CI, 1.02-1.73). In a multivariable‑adjusted analysis, the use of BZD was independently associated with increased death risk (HR, 1.36; 95% CI, 1.06-1.75).CONCLUSIONSThe patients medicated with BZD presented a 36% higher risk of dying. BZD should probably be used with caution, particularly in older HF patients and in those with CKD.</description><identifier>EISSN: 1897-9483</identifier><identifier>DOI: 10.20452/pamw.16464</identifier><language>eng</language><ispartof>Polskie archiwum medycyny wewne̦trznej, 2023-10, Vol.133 (10)</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Ribeirinho-Soares, Pedro</creatorcontrib><creatorcontrib>Madureira, Sérgio</creatorcontrib><creatorcontrib>Elias, Catarina</creatorcontrib><creatorcontrib>Gouveia, Rita</creatorcontrib><creatorcontrib>Neves, Ana</creatorcontrib><creatorcontrib>Amorim, Marta</creatorcontrib><creatorcontrib>Carreira, Marta S</creatorcontrib><creatorcontrib>Pereira, Joana</creatorcontrib><creatorcontrib>Almeida, Jorge</creatorcontrib><creatorcontrib>Lourenço, Patrícia</creatorcontrib><title>Benzodiazepine use and mortality in chronic heart failure</title><title>Polskie archiwum medycyny wewne̦trznej</title><description>INTRODUCTIONThe prognostic implications of using benzodiazepines (BZD) in heart failure (HF) patients are still unknown.OBJECTIVESThis study aimed to assess the association of BZD use with all‑cause death in ambulatory, chronic HF patients.PATIENTS AND METHODSWe investigated a retrospective cohort of ambulatory HF patients with left ventricular systolic dysfunction (LVSD). The patients were followed up from their first medical appointment until January 2021 and all‑cause mortality was the primary end point. The Cox regression analysis was used to assess the association between BZD use and all‑cause mortality. Subgroup analyses were performed considering age, sex, body mass index (BMI), respiratory disease, chronic kidney disease (CKD), and New York Heart Association (NYHA) class. Multivariable models were built to account for confounders.RESULTSWe studied 854 patients (69% men), of mean (SD) age 71 (13) years, of whom 51% had severe LSVD, and 242 (28.3%) regularly used BZD. During a median follow‑up of 46 months, 443 patients (51.9%) died. BZD use predicted no crude survival disadvantage in the entire investigated group and in the subgroup analysis according to sex, respiratory disease, BMI, and NYHA class. BZD use was not mortality‑associated among patients aged 75 years and younger. However, in those older than 75 years the hazard ratio (HR) of all‑cause death was 1.3 (95% CI, 0.99-1.69; P = 0.06). BZD use seemed safe in the patients without CKD, but in those with CKD it was associated with worse survival (HR, 1.33; 95% CI, 1.02-1.73). In a multivariable‑adjusted analysis, the use of BZD was independently associated with increased death risk (HR, 1.36; 95% CI, 1.06-1.75).CONCLUSIONSThe patients medicated with BZD presented a 36% higher risk of dying. 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The patients were followed up from their first medical appointment until January 2021 and all‑cause mortality was the primary end point. The Cox regression analysis was used to assess the association between BZD use and all‑cause mortality. Subgroup analyses were performed considering age, sex, body mass index (BMI), respiratory disease, chronic kidney disease (CKD), and New York Heart Association (NYHA) class. Multivariable models were built to account for confounders.RESULTSWe studied 854 patients (69% men), of mean (SD) age 71 (13) years, of whom 51% had severe LSVD, and 242 (28.3%) regularly used BZD. During a median follow‑up of 46 months, 443 patients (51.9%) died. BZD use predicted no crude survival disadvantage in the entire investigated group and in the subgroup analysis according to sex, respiratory disease, BMI, and NYHA class. BZD use was not mortality‑associated among patients aged 75 years and younger. However, in those older than 75 years the hazard ratio (HR) of all‑cause death was 1.3 (95% CI, 0.99-1.69; P = 0.06). BZD use seemed safe in the patients without CKD, but in those with CKD it was associated with worse survival (HR, 1.33; 95% CI, 1.02-1.73). In a multivariable‑adjusted analysis, the use of BZD was independently associated with increased death risk (HR, 1.36; 95% CI, 1.06-1.75).CONCLUSIONSThe patients medicated with BZD presented a 36% higher risk of dying. BZD should probably be used with caution, particularly in older HF patients and in those with CKD.</abstract><doi>10.20452/pamw.16464</doi><oa>free_for_read</oa></addata></record>
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title Benzodiazepine use and mortality in chronic heart failure
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